Just wanted to up date my input: My Wife & I have just put in the one month upate to her CCSVI Tracking page and with the exception of the walking / balance section (the sprained ankle is still not properly healed so it is still causing problems in both these areas) pretty much everything else was an improvement. I really feel she answered the questions honestly and I could certainly verify a lot of her responses. Once the information is given, you can get a graph of the tracked input - it was so good to see "Quality of Life" getting better, because that's one of the really important questions, and the one that makes the decision, the expense of CCSVI treatment, worth it all.

I mentioned the CCSVI Tracking site as being important to the MS / CCSVI "culture", but it really is a fantastic tool to be able to see what's happening. So again, if you're going for treatment, if you've been for treatment, join the CCSVI Tracking site and not only share your information (good or bad - everyone needs to know if this treatment is the "real thing" or not) but also keep your own personal graph for yourself.